Classifications

• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D501/00—Heterocyclic compounds containing 5-thia-1-azabicyclo [4.2.0] octane ring systems, i.e. compounds containing a ring system of the formula:, e.g. cephalosporins; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulfur-containing hetero ring
  • C07D501/14—Compounds having a nitrogen atom directly attached in position 7
  • C07D501/16—Compounds having a nitrogen atom directly attached in position 7 with a double bond between positions 2 and 3
  • C07D501/20—7-Acylaminocephalosporanic or substituted 7-acylaminocephalosporanic acids in which the acyl radicals are derived from carboxylic acids
  • C07D501/24—7-Acylaminocephalosporanic or substituted 7-acylaminocephalosporanic acids in which the acyl radicals are derived from carboxylic acids with hydrocarbon radicals, substituted by hetero atoms or hetero rings, attached in position 3
  • C07D501/36—Methylene radicals, substituted by sulfur atoms
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D501/00—Heterocyclic compounds containing 5-thia-1-azabicyclo [4.2.0] octane ring systems, i.e. compounds containing a ring system of the formula:, e.g. cephalosporins; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulfur-containing hetero ring
  • C07D501/14—Compounds having a nitrogen atom directly attached in position 7
  • C07D501/16—Compounds having a nitrogen atom directly attached in position 7 with a double bond between positions 2 and 3
  • C07D501/20—7-Acylaminocephalosporanic or substituted 7-acylaminocephalosporanic acids in which the acyl radicals are derived from carboxylic acids
  • C07D501/24—7-Acylaminocephalosporanic or substituted 7-acylaminocephalosporanic acids in which the acyl radicals are derived from carboxylic acids with hydrocarbon radicals, substituted by hetero atoms or hetero rings, attached in position 3
  • C07D501/26—Methylene radicals, substituted by oxygen atoms; Lactones thereof with the 2-carboxyl group
  • C07D501/34—Methylene radicals, substituted by oxygen atoms; Lactones thereof with the 2-carboxyl group with the 7-amino radical acylated by carboxylic acids containing hetero rings
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
  • Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
  • Y02P20/00—Technologies relating to chemical industry
  • Y02P20/50—Improvements relating to the production of bulk chemicals
  • Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups

Definitions

• This invention relates to a novel ⁇ -lactam compound, more particularly to a novel cephalosporin series compound useful for antibiotics, a method for preparing the same, a synthetic intermediate and use thereof.
• the present inventors have intensively studied, by referring to the above situation, concerning a compound which has potent antibacterial activities in extremely wide ranges, and as a result, have found that the compound represented by the formula (I) has excellent characteristics as a medicinal composition for bacterially infectious disease (microbism) therapy and accomplished the present invention.
• the present invention relates to a ⁇ -lactam compound represented by the formula (I): ##STR2##
• R 1 and R 2 are independently a hydrogen atom or a lower alkyl group
• M is a hydrogen atom, a protective group or an eliminatable group which is easily hydrolyzable in a human body
• R' and R" are independently represent a hydrogen atom or a protective group
• A is a mercapto group which is substituted by a substituted or unsubstituted polycyclic nitrogen-containing heterocyclic ring or a group represented by the following formula (a):
• R 3 and R 4 are independently a hydrogen atom or an lower alkyl group, provided that when R 1 and R 2 are both hydrogen atoms, both R 3 and R 4 being hydrogen atoms are excluded), or its pharmaceutically acceptable salt, a method for preparing the same, a synthetic intermediate thereof and a medicinal composition for microbism therapy containing said compound as its active ingredient.
• R 1 and R 2 are independently a hydrogen atom or a lower alkyl group.
• R' is a hydrogen atom or a protective group.
• the lower alkyl group includes straight or branched alkyl groups having 1 to 3 carbon atoms such as a methyl group, an ethyl group, an n- or iso-propyl group, etc.
• the protective group represented by R' includes a diphenylmethyl group, a t-butyl group, a p-nitrobenzyl group, a trimethylsilyl group, etc.
• the protective group there may be mentioned, for example, a lower acyl group such as an acetyl group, a propionyl group, etc.; and a lower alkoxycarbonyl group such as a methoxycarbonyl group, an ethoxycarbonyl group, etc.
• M is a hydrogen atom, a protective group or an eliminable group which is easily hydrolyzable in a human body.
• the M is a protective group
• a diphenylmethyl group a t-butyl group, a p-nitrobenzyl group, a trimethylsilyl group, etc.
• the M is an eliminable group which is easily hydrolyzable in a human body
• an acetoxymethyl group an ⁇ -acetoxyethyl group, a pivaroyloxymethyl group, an ⁇ -ethoxycarbonyloxymethyl group, an ⁇ -methoxycarbonyloxymethyl group, an ⁇ -methoxycarbonyloxyethyl group, an ⁇ -ethoxycarbonyloxyethyl group, a 1-indanyl group, a phthalidyl group, a 5-methyl-2-oxo 1,3-dioxol-4-yl-methyl group and the like.
• the A may be a mercapto group substituted by a substituted or unsubstituted polycyclic nitrogen-containing heterocyclic ring.
• a mercapto group substituted by a heterocyclic ring may be mentioned, for example, the following formula (b), (c), or (d) or (e): ##STR3##
• R 5 , R 6 , R 7 , R 8 , R 9 , R 10 , R 11 , R 12 and R 13 represent independently a hydrogen atom, a lower alkyl group which may be substituted by a halogen atom, a cycloalkyl group or a carboxyl group which may be substituted by a protective group or an eliminatable group which is easily hydrolyzable in a human body and further, R 7 and R 8 , R 10 and R 11 , and R 12 and R 13 may be combined with each other, respectively, to form an alky
• the lower alkyl group which may be substituted by a halogen atom there may be mentioned, for example, a methyl group, an ethyl group, an n- or iso-propyl group, a monofluoromethyl group, a difluoromethyl group, a trifluoromethyl group, a monofluoroethyl group, a difluoroethyl group, a trifluoroethyl group, etc.
• the cycloalkyl group may include, for example, a cyclopropyl group, a cyclobutyl group, a cyclopentyl group, a cyclohexyl group, etc.
• the protective group and the eliminatable group in the carboxyl group which may be substituted by the protective group or the eliminable group which is easily hydrolyzable in a human body have the same meanings as the groups defined above as the M.
• the alkylene group having 3 to 4 carbon atoms may include, for example, a propylene group, a butylene group etc.
• alkali metal salts such as of sodium salts, potassium salts, etc.
• alkaline earth metal salts such as of magnesium salts, calcium salts, etc.
• ammonium salts salts with organic bases such as of diisopropylamine, benzylamine, triethanolamine, triethylamine, N-methylmorpholine, pyridine, piperazine, etc.
• salts with organic acids such as of acetic acid, formic acid, maleic acid, fumaric acid, methanesulfonic acid, p-toluenesulfonic acid, etc.
• salts with inorganic acids such as of hydrochloric acid, hydrobromic acid, sulfuric acid, phosphoric acid and the like.
• novel ⁇ -lactam compounds to be intended in the present invention can be synthesized according to the following three methods.
• the first method is the first method.
• the title compound can be obtained by reacting the compound represented by the formula (II): ##STR4## wherein symbols in the formula are the same as mentioned above, with the carboxylic acid represented by the formula (III): ##STR5## wherein symbols in the formula are the same as mentioned above, or its reactive derivative and removing a protective group, if necessary.
• the title compound can be obtained by reacting the compound represented by the formula (IV): ##STR7## wherein symbols in the formula are the same as mentioned above, with the compound represented by the formula (V): ##STR8## or its reactive derivative and removing a protective group, if necessary.
• the starting compound represented by the formula (IV) is a novel compound, and an example of the synthesizing method is shown by referring reaction schemes in the following: ##STR9## wherein R" is a protective group and the other symbols are the same as mentioned above.
• the first method is the first method.
• the reaction between the compound (Il) and the compound (III) should desirably be carried out, in general, by using reactive derivatives of the compound (III) as the compound (III).
• reactive derivatives there may be mentioned, for example, acid halides, mixed acid anhydrides, active esters and the like.
• suitable condensation reagent may desirably be used in this case.
• reagent there may be employed, for example, N,N'-dicyclohexylcarbodiimide (DCC), N,N'-carbonyldiimidazole, cyanuric chloride, Vilsmeier reagent and the like.
• DCC N,N'-dicyclohexylcarbodiimide
• N,N'-carbonyldiimidazole N,N'-carbonyldiimidazole
• cyanuric chloride cyanuric chloride
• Vilsmeier reagent equimolar amounts of the compounds (II) and (III) are employed in general.
• reaction are usually carried out at -10° to 30° C. for about 0.5 to 2 hours in a suitable solvent such as methylene chloride, chloroform, tetrahydrofuran, dioxane, dimethylformamide, dimethylacetamide, acetonitrile, acetone, water or mixed solvents of the above.
• a suitable solvent such as methylene chloride, chloroform, tetrahydrofuran, dioxane, dimethylformamide, dimethylacetamide, acetonitrile, acetone, water or mixed solvents of the above.
• Treatments after the reaction can be carried out by the methods well known in the art such as separation, purification and the like.
• reaction of the compound (IV) and ##STR12## is carried out by allowing the latter as such or the hydroxyl group protected as an acyl ester to react as acid halides, mixed acid anhydrides or active esters, or suitable condensation reagents such as N,N'-dicyclohexylcarbodiimide (DCC), N,N'-carbonyldiimidazole, cyanuric chloride, Vilsmeier reagent and the like can be employed.
• suitable condensation reagents such as N,N'-dicyclohexylcarbodiimide (DCC), N,N'-carbonyldiimidazole, cyanuric chloride, Vilsmeier reagent and the like can be employed.
• the compounds represented by the formula (VII) may include, for example, the following compounds:
• the reaction of the compound (VI) and the compound (VII), is carried out by contacting them in water or water and a water-soluble organic solvent such as acetone, methanol, ethanol, isopropanol, acetonitrile, etc.
• a water-soluble organic solvent such as acetone, methanol, ethanol, isopropanol, acetonitrile, etc.
• --COOM is a free carboxylic acid or its salt.
• This reaction is desirably carried out at around neutral of pH and the reaction system can be maintained at around neutral by properly adding alkaline compounds such as an alkali hydroxide, an alkali carbonate, an alkali hydrogencarbonate, an alkali dihydrogenphosphate, an alkali monohydrogenphosphate, etc.
• the reaction temperature is generally about 20° to 70° C.
• the terminal point of the reaction is confirmed by a thin layer chromatography.
• the reaction time is about 0.5 to 24 hours. Since the thus obtained compound (I') is being dissolved as a water-soluble alkali salt in a reaction mixture, an adsorption, separation and purification are carried out by using adsorptive resins such as Diaion HP-20 (trade name, produced by Mitsubishi Kasei Co.), Amberlite XAD II (trade name, produced by Rohm & Haas, Co.) etc.
• adsorptive resins such as Diaion HP-20 (trade name, produced by Mitsubishi Kasei Co.), Amberlite XAD II (trade name, produced by Rohm & Haas, Co.) etc.
• the reaction is carried out in an organic solvent such as methanol, ethanol, isopropanol, tetrahydrofuran, acetonitrile, dimethylformamide and the like at 50° to 100° C for 0.5 to 3 hours.
• organic solvent such as methanol, ethanol, isopropanol, tetrahydrofuran, acetonitrile, dimethylformamide and the like at 50° to 100° C for 0.5 to 3 hours.
• the equimolar amounts of the compound (VI) and the compound (VII) are generally employed, respectively.
• the compound represented by the formula (I) or its pharmaceutically acceptable salt can also be prepared by reacting a compound represented by the formula (XI): ##STR13## wherein R' and A are the same meanings as defined above, with the compound represented by the formula (XII): ##STR14## wherein R 1 and R 2 have the same meanings as defined above, or with a salt thereof.
• the reaction involving compounds of the formula (XI) is preferably carried out by using a salt of the compound of the formula (XII).
• a salt of the compound of the formula (XII) preferably salts with mineral acids are employed, e.g., the hydrochlorides, or an organic sulfonate, e.g., the p-toluene sulfonates.
• the salt is preferably employed in about equimolar amounts up to slight excess thereof.
• the reaction is preferably carried out in a polar organic solvent, e.g., dimethylformamide, N-methylpyrrolidone, dimethylsulfoxide, acetonitrile, water or, particularly preferred, in dimethylacetamide. When using this latter solvent particularly high amounts of the syn form of the end products are obtained.
• the temperature of the reaction preferably lies in the range between 0° C. and room temperature.
• the compound (I) obtained by each methods of (1), (2), and (3) as mentioned above can be converted into, if necessary, a pharmaceutically acceptable salt or an ester which is easily hydrolyzed in a human body when the compound has a free carboxylic acid.
• the ⁇ -lactam compound according to the present invention can be administrated orally or non-orally to human beings or animals by various known administrating method.
• said compounds are used singly or by formulating with auxiliaries, liquid diluents, binders, lubricants, humectants, etc., which are pharmaceutically acceptable in general, for example, in the form of general medicinal compositions such as tablets, granulars, sugar coating tablets, powder, capsules, gels, dry syrup, syrup, amples, suspension, liquid, emulsion, ointments, paste, cream, suppositories, etc.
• auxiliaries liquid diluents, binders, lubricants, humectants, etc.
• dissolution delaying agents there may be mentioned dissolution delaying agents, adsorption accelerating agents, surface active agents, etc. Any way, any forms which are pharmaceutically acceptable can be employed.
• the ⁇ -lactam compound according to the present invention can be used as alone or mixture of two or more different kinds of derivatives and the amount of the compounds is about 0.1 to 99.5%, preferably 0.5 to 95% based on the weight of the all medicinal composition.
• the medicinal composition containing the compound of the present invention can be formulated with an other compounds which are pharmaceutically active as effective ingredients other than said compound or mixtures thereof.
• a dosage per day to a patient of the novel ⁇ -lactam compound according to the present invention may be varied depending upon an individual man, kinds of animals, weights thereof and a state to be remedied, but generally is in the range of 1 to 1000 mg per 1 kg of weight, preferably about 10 to 800 mg.
• the compound of the above formula (I) obtained according to the present invention has high antibacterial activity as well as no toxicity at an effective dosage LD 50 value is 2 g/kg when intraveneous administration to mouse is carried out) and thus it is an effective compound as a medicine.
• it shows excellent antibacterial activity against a wide range of pathogenic bacteria such as gram negative bacteria including Pseudomonas aeruginosa and gram positive bacteria.
• the compound of the present invention is effective to a part of the third aged cephalosporin resistance acquired strains when administration thereof is carried out.
• the ⁇ -lactam compound according to the present invention can be effectively utilized for the sake of prevention or remedy of diseases due to the aforesaid pathogenic bacteria in human beings or animals.
• Example 1 20 mg/kg of the compound obtained in Example 1 was administered parenterally to Macaco and a central distribution volume and a tissue distribution volume were calculated by their concentrations in blood measured with time. The results are shown in Table 1.
• the concentration of the compound was measured according to HPLC method.
• Microbondapack C18 (trade name, produced by Waters Co.) was used as a column and 8% acetonitrile-2% tetrahydrofuran-0.2% phosphoric acid was used as a solvent.
• the minimum inhibition concentrations (MIC) of the compounds obtained in Example 1 and Example 2 were measured according to the standard method of Japanese Chemotherapy Association. The results are shown in Table 2 and Table 3.
• the compounds of the present invention are effective to gram positive bacteria and gram negative bacteria and have wide range of antibacterial spectrum.
• EXAMPLE 12 7- ⁇ 2-[2-Amino-1,3-thiazol-4-yl]-2-[1-(3-(3,4-dihydroxybenzoyl)carbazoyl)-1-methylethoxyimino]acetamide ⁇ -3-[(5-methyl-s-triazolo[1,5-a]-pyrimidin-7-yl)thiomethyl]-3-cephem-4-carboxylic acid.hydrochloride
• the reaction mixture was ice-cooled and then poured into 400 ml of water.
• the pH of the mixture was adjusted to 2 with concentrated ammonia water and the crystals precipitated were collected by filtration and washed with water, acetone and then ether, followed by drying, to obtain 25 g of the title compound (Yield: 66%).
• the reaction mixture was ice-cooled and then poured into 300 ml of water.
• the pH of the mixture was adjusted to about 2.5 with concentrated aqueous ammonia and the precipitates were collected by filtration and washed with water and then acetone, followed by drying, to obtain 9.98 g of the title compound (Yield: 70.9%).
• Example 25 Each of 20 mg/kg of the compounds obtained in Example 2, Example 25 and Example 28 was administered parenterally to Macaco and the half-time in blood was measured. The results are shown in Table 4.
• the concentrations of the compounds were measured according to HPLC method. Novapack C18 or Microbondapack C18 (trade name, produced by Waters Co.) was used as a column. Further, cefpiramide was used as a control drug.
• the half-times in blood of the compounds according to the present invention are longer than that of cefpiramide in the case of Macaco.
• cefpiramide is known as a cephalosporin having a long prolonged time in blood.
• the results in Table 4 suggest that the half-times in blood of said compounds are longer than that of cefpiramide in the case of human beings. High usefulness such that the same or higher clinical effect is obtained with a smaller number of administration, when compared with other medicines, can be expected.
• the minimum inhibition concentrations (MIC) of the compounds obtained in the respective examples described above were measured according to the standard method of Japanese Chemotherapy Association. The results are shown in Table 5 and Table 6.
• cephazoline (CAZ) was used as a control compound.
• the compounds of the present invention is effective to gram positive bacteria and gram negative bacteria and have wide range of antibacterial spectrum.
• the compounds of the present invention exhibit strong antibacterial activities to glucose non-fermentable bacteria including Pseudomonas aeruginosa when compared with those of the third aged series cephalosporin.
• the compounds of the present invention exhibit strong antibacterial activities to a cephazoline resistance clinical separated strain which is one of the third aged series cephalosporins.
• Example 25 In the same manner as in Example 25, the compounds of Examples 54, 57 and 58, and in the same manner as in Example 37, the compounds of Examples 55 and 56 were prepared, respectively.
• the product is 7- ⁇ 2-[2-amino-1,3-thiazol-4-yl]-2-[1-(3-(3,4-dihyroxybenzoyl)carbozoyl)-1-methylethoxy]imino]-acetamido ⁇ -3-[(2-carboxy-5-methyl-s-triazolo[1,5-a]pyrimidin-7-yl]thiomethyl]-3-cephem-4-carboxylic acid.
• This produce (2.07 g) was dissolved in 20 ml of dimethylformamide and 20 ml of ethanol. A 2N solution of sodium-2-ethylcaproate in acetone (3 ml) was added. The precipitated disodium salt was collected, washed with ethanol and n-hexane and dried in vacuo at 30° C.
• the mixture was stirred for 4 hours at 60° C. After cooling, the mixture was poured into 6 liters of water and the product was extracted with 3 liters of ethyl acetate. After washing twice with 0.5 liter of a sodium chloride solution, the solvent was evaporated and the residue was recrystallized from 0.6 liter of tert-butyl methyl ether and 1.5 liters of hexane to obtain the product, m.p. 51°-53° C.
• the allyl ester (187.6 g) which was obtained in Step 1 was dissolved in 1.5 liters of acetonitrile. After addition of 1 g of palladium-(II)-acetate, 6.5 ml of triethylphosphite and 62.4 g of N-methylpyrrolidine, the mixture was stirred for 2 hours at room temperature. The solvent was evaporated, and the residue was partitioned between 0.5 liter of water and 0.5 liter of ethyl acetate. The aqueous phase was then adjusted to pH 3-4 with 150 ml of 3N aqueous HCl. After cooling, the product was filtered. m.p. 133°-135° C.
• the product was 7- ⁇ 2-[2-amino-1,3-thiazol-4-yl]-2-[1(3 -(2,3-dihydroxybenzoly)carbazoyl]-1-methylethoxyimino]acetamido ⁇ -3-[(2-carboxy-5-methyl-s-triazolo[1,5-a]pyrimidin-7-yl)thiomethyl]-3-cephem-4-carboxylic acid.
• the 1-(2-aminooxy-2-methylpropionyl)-2-(2,3-dihydroxybenzoyl)hydrazine.hydrochloride can be prepared from 2,3-dihydroxybenzoic acid in analogy to Example 59. Melting point: 208°-211° C. (decomposed).
• the minimum inhibition concentrations (MIC) of the compounds obtained in the respective examples described above were measured according to the standard method of Japanese Chemotherapy Association. The results are shown in Table 7 and Table 8.
• the compounds of the present invention is effective to gram positive bacteria and gram negative bacteria and have wide range of antibacterial spectrum.
• the compounds of the present invention exhibit strong antibacterial activities to glucose non-fermentable bacteria including Pseudomonas aeruginosa when compared with those of the third aged series cephalosporin.
• the compounds of the present invention exhibit strong antibacterial activities against a cephazoline resistance clinical separated strain which is one of the third aged series cephalosporins.

Landscapes

• Chemical & Material Sciences (AREA)
• Organic Chemistry (AREA)
• Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
• Nitrogen Condensed Heterocyclic Rings (AREA)
• Cephalosporin Compounds (AREA)

Applications Claiming Priority (4)

Publications (1)

Family

ID=26493073

Family Applications (1)

Country Status (17)

Cited By (1)

Families Citing this family (14)

Citations (7)

Family Cites Families (3)

• 1987
  • 1987-06-30 FI FI872879A patent/FI872879A/fi not_active Application Discontinuation
  • 1987-07-13 NZ NZ221052A patent/NZ221052A/xx unknown
  • 1987-07-15 IL IL83194A patent/IL83194A0/xx unknown
  • 1987-07-17 MC MC881900A patent/MC1838A1/fr unknown
  • 1987-07-17 EP EP87306330A patent/EP0254495A3/fr not_active Withdrawn
  • 1987-07-17 ZW ZW133/87A patent/ZW13387A1/xx unknown
  • 1987-07-17 HU HU873267A patent/HU198944B/hu unknown
  • 1987-07-20 OA OA59168A patent/OA08639A/xx unknown
  • 1987-07-20 DK DK378187A patent/DK378187A/da not_active Application Discontinuation
  • 1987-07-20 MA MA21280A patent/MA21148A1/fr unknown
  • 1987-07-20 US US07/075,412 patent/US4966900A/en not_active Expired - Fee Related
  • 1987-07-20 PH PH35560A patent/PH25108A/en unknown
  • 1987-07-20 KR KR1019870007818A patent/KR880001677A/ko not_active Application Discontinuation
  • 1987-07-20 AU AU75917/87A patent/AU597695B2/en not_active Ceased
  • 1987-07-21 CN CN198787104995A patent/CN87104995A/zh active Pending
  • 1987-07-21 PT PT85375A patent/PT85375B/pt not_active IP Right Cessation
  • 1987-08-19 TN TNTNSN87101A patent/TNSN87101A1/fr unknown
• 1988
  • 1988-06-09 MC MC88210K patent/MC210A7/fr unknown

Patent Citations (7)

Non-Patent Citations (2)

Also Published As

Similar Documents

Legal Events